Izon D J, Punt J A, Xu L, Karnell F G, Allman D, Myung P S, Boerth N J, Pui J C, Koretzky G A, Pear W S
Department of Pathology and Laboratory Medicine, University of Pennsylvania Medical Center, Philadelphia, PA 19104, USA.
Immunity. 2001 Mar;14(3):253-64. doi: 10.1016/s1074-7613(01)00107-8.
Notch signaling regulates cell fate decisions in multiple lineages. We demonstrate in this report that retroviral expression of activated Notch1 in mouse thymocytes abrogates differentiation of immature CD4+CD8+ thymocytes into both CD4 and CD8 mature single-positive T cells. The ability of Notch1 to inhibit T cell development was observed in vitro and in vivo with both normal and TCR transgenic thymocytes. Notch1-mediated developmental arrest was dose dependent and was associated with impaired thymocyte responses to TCR stimulation. Notch1 also inhibited TCR-mediated signaling in Jurkat T cells. These data indicate that constitutively active Notch1 abrogates CD4+ and CD8+ maturation by interfering with TCR signal strength and provide an explanation for the physiological regulation of Notch expression during thymocyte development.
Notch信号通路调控多个谱系中的细胞命运决定。我们在本报告中证明,在小鼠胸腺细胞中逆转录病毒表达活化的Notch1可消除未成熟CD4+CD8+胸腺细胞向CD4和CD8成熟单阳性T细胞的分化。在体外和体内,无论是正常胸腺细胞还是TCR转基因胸腺细胞,都观察到了Notch1抑制T细胞发育的能力。Notch1介导的发育停滞呈剂量依赖性,并且与胸腺细胞对TCR刺激的反应受损有关。Notch1还抑制Jurkat T细胞中TCR介导的信号传导。这些数据表明,组成型活性Notch1通过干扰TCR信号强度消除CD4+和CD8+的成熟,并为胸腺细胞发育过程中Notch表达的生理调节提供了解释。